| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6390637-6390889 | Common:6; Rare:120; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr11:6419028-6419199 | Common:2; Rare:39 | ||||
| chr11:6473812-6474084 | Rare:84 | ||||
| chr11:6481231-6481558 | Common:5; Rare:140 | ||||
| chr11:6603550-6603864 | Common:4; Rare:91; Clinvar (benign):3 | ||||
| chr11:6603970-6604075 | Common:1; Rare:30 | ||||
| chr11:6682943-6683437 | Common:3; Rare:195 | ||||
| chr11:6926364-6926598 | Common:5; Rare:71 | ||||
| chr11:6926846-6926887 | Rare:11 | ||||
| chr11:7020310-7020493 | Rare:65 | ||||
| chr11:7965436-7965660 | Common:2; Rare:31 | ||||
| chr11:7991475-7991778 | Rare:69 | ||||
| chr11:7994424-7994599 | Rare:63; Clinvar (pathogenic):1 | ||||
| chr11:8682637-8683317 | Common:4; Rare:265 | ||||
| chr11:8717808-8717950 | Common:1; Rare:43 |